Canonical Allele Identifier: CA2392518519

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138627_46138629delinsCCT , CM000683.2:g.46138627_46138629delinsCCT	GRCh38
NC_000021.8:g.47558541_47558543delinsCCT , CM000683.1:g.47558541_47558543delinsCCT	GRCh37
NC_000021.7:g.46382969_46382971delinsCCT	NCBI36
NG_016191.1:g.21939_21941delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-143_-141delinsAGG	ENSP00000507070.1:n.-143_-141delinsAGG
ENST00000494498.2:c.56_58delinsAGG	ENSP00000507847.1:p.Gln19=
ENST00000397746.8:c.1322_1324delinsAGG MANE Select	ENSP00000380854.3:p.Gln441=
ENST00000291670.9:c.1322_1324delinsAGG	ENSP00000291670.5:p.Gln441=
ENST00000397743.1:c.1278_1280delinsAGG	ENSP00000380851.1:p.Thr426=
ENST00000397746.7:c.1322_1324delinsAGG	ENSP00000380854.3:p.Gln441=
ENST00000397748.5:c.1322_1324delinsAGG	ENSP00000380856.1:p.Gln441=
ENST00000460011.5:n.651_653delinsAGG
ENST00000488577.1:n.348_350delinsAGG
ENST00000494498.1:n.623_625delinsAGG
ENST00000498355.6:n.1391_1393delinsAGG
NM_006657.2:c.1322_1324delinsAGG	NP_006648.1:p.Gln441=
NM_206965.1:c.1322_1324delinsAGG	NP_996848.1:p.Gln441=
XM_006723961.2:c.1571_1573delinsAGG	XP_006724024.2:p.Gln524=
XM_006723962.2:c.1571_1573delinsAGG	XP_006724025.2:p.Gln524=
XM_011529434.1:c.1571_1573delinsAGG	XP_011527736.1:p.Gln524=
XM_011529435.1:c.1442_1444delinsAGG	XP_011527737.1:p.Gln481=
XM_011529436.1:c.1571_1573delinsAGG	XP_011527738.1:p.Gln524=
XM_011529437.1:c.1571_1573delinsAGG	XP_011527739.1:p.Gln524=
XM_011529438.1:c.1442_1444delinsAGG	XP_011527740.1:p.Gln481=
XM_011529439.1:c.1058_1060delinsAGG	XP_011527741.1:p.Gln353=
XR_937433.1:n.1754_1756delinsAGG
NM_001320412.1:c.1322_1324delinsAGG	NP_001307341.1:p.Gln441=
XM_006723961.4:c.1571_1573delinsAGG	XP_006724024.2:p.Gln524=
XM_006723962.4:c.1571_1573delinsAGG	XP_006724025.2:p.Gln524=
XM_011529434.3:c.1571_1573delinsAGG	XP_011527736.1:p.Gln524=
XM_011529435.3:c.1442_1444delinsAGG	XP_011527737.1:p.Gln481=
XM_011529436.3:c.1571_1573delinsAGG	XP_011527738.1:p.Gln524=
XM_011529437.3:c.1571_1573delinsAGG	XP_011527739.1:p.Gln524=
XM_011529439.2:c.1058_1060delinsAGG	XP_011527741.1:p.Gln353=
XR_937433.3:n.1788_1790delinsAGG
NM_206965.2:c.1322_1324delinsAGG MANE Select	NP_996848.1:p.Gln441=
NM_001320412.2:c.1322_1324delinsAGG	NP_001307341.1:p.Gln441=
NM_006657.3:c.1322_1324delinsAGG	NP_006648.1:p.Gln441=